|
Operational
|
2002
|
|
Source characteristics
|
Superbend
|
|
Energy range
|
6-18 keV
|
|
Monochromator #1
|
Double crystal
|
|
Calculated flux (1.9 GeV, 400 mA)
|
5 x 1011 photons/s (100 µm collimator)
|
|
Resolving power (E/DE)
|
7000
|
|
Monochromator #2
|
Double multilayer
|
|
Calculated flux (1.9 GeV, 400 mA)
|
4 x 1013 photons/s
|
|
Resolving power (E/DE)
|
100
|
|
Endstations
|
Hutch
|
|
Detectors
|
Monochromator #1: 2 x 2 array CCD
Monochromator #2: Fast wire chamber
|
|
Calculated spot size at sample (FWHM)
|
Monochromator #1: 65 x 150 µm
Monochromator #2: 6 x 1 mm
|
|
Samples
|
|
Format
|
Monochromator #1: Single-crystal biomolecules
Monochromator #2: Solutions
|
|
Preparation
|
Support labs available
|
|
Sample environment
|
Monochromator #1: Cryofrozen crystals
Monochromator #2: Liquid cell
|
|
Special notes
|
Computers for data processing and analysis are available
|
|
Scientific applications
|
Biological crystallography; multiple-wavelength anomalous diffraction (MAD), small-angle x-ray scattering (SAXS)
|
|
Local contact
|
Name: Howard Padmore
Phone: (510) 486-5787
Fax: (510) 486-7696
Email: hapadmore@lbl.gov
|
|
Spokesperson
|
Name: John Tainer
Affiliation: The Scripps Research Institute
Phone: (858) 784-8119
Fax: (858) 784-2277
Email: jat@scripps.edu
|